Leonhard Lang Gmbh: Medical Device Recall in 2014 - (Recall #: Z-0802-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

GE Healthcare Pediatric Direct-Wired Disposable Defibrillation/Pacing Electrodes. REF 2059144-001 and 2059144-005. . Product Usage: Usage: Skintact Pediatric Multifunction Electrodes are for use on pediatric patients, less than 8 years of age, or weighing less than 25 kg (55 lbs), for external defibrillation, pacing, monitoring and cardioversion. The device is non-sterile and for single use only.

Product Classification:

Class I

Date Initiated: December 3, 2014

Date Posted: December 31, 2014

Recall Number: Z-0802-2015

Event ID: 69930

Reason for Recall:

The firm discovered that during the use of these defibrillation electrodes a possibility for arcing and a resulting malfunction exists. This could lead to a situation, in which a patient who is in a life threatening situation requiring a defibrillation can receive such therapy only with a delay or not at all.

Status: Terminated

Product Quantity: 1080 pieces

Code Information:

Lots: 30618-0771, 30702-0778, 40217-0776, 40407-0777, 40424-0772, 40704-0775

Distribution Pattern:

US Nationwide Distribution in the states of OH and TX.

Voluntary or Mandated:

Voluntary: Firm initiated